在对痴呆症护理中的不良行为进行管理时,预防安置破裂和入院风险:与家庭和护理院工作人员共同开展的定性案例研究。

Katherine Nunn, Suzanne Crooks, Donna Gilroy
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引用次数: 0

摘要

目的:打人和拒绝个人护理等行为是痴呆症患者的常见表现,与护理人员的压力和焦虑以及护理之家的安置中断有关。传统上,人们使用药物方法来控制行为,但研究表明,这种方法的效果有限。国家指导方针建议将非药物干预作为治疗困扰的第一线方法,但还需要进一步的研究来阐明改善痴呆症患者护理的要素。本研究旨在通过案例研究,探讨非药物临床干预--"纽卡斯尔模式"--在护理院环境中用于理解和管理痴呆症护理中的困扰行为的有效方法。研究方法采用定性案例研究设计。从爱丁堡行为支持服务机构中选取了三个案例,因为这些案例在苏格兰国家医疗服务体系(NHS)的不良行为干预过程中成功地防止了护理院安置破裂。对这些案例中参与干预的家庭成员和工作人员进行了访谈(N = 6)。采用主题分析法对数据进行分析。研究结果所有参与者都报告了干预的积极成果。确定了三个关键主题,每个主题都有副主题。参与者描述了一种支持性的、不做评判的环境,这种环境使他们能够整合有关痴呆症的知识,并根据痴呆症患者的具体需求制定干预措施。此外,他们还感受到了家人和员工齐心协力、为共同目标而奋斗的精神。本文介绍了所有主题及其互动的初步模型。结论:这项研究支持在社区护理环境中使用以生物心理社会学为主导的方法来理解和治疗复杂的行为表现。研究建议临床医生应努力为护理院工作人员和家庭成员营造安全、开放的环境,以促进归因改变和以人为本的护理,并帮助调解工作人员和家庭成员之间的分歧和冲突。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Preventing risk of placement breakdown and hospital admission in the management of distressed behaviour in dementia care: A qualitative case study with family and care-home staff.

Objectives: Behaviours such as hitting-out and declining personal care are commonly exhibited by people living with dementia and are associated with care-giver stress and anxiety and care home placement breakdowns. Traditionally, pharmacological approaches have been used to manage behaviour; however, research indicates limited effectiveness. National guidelines recommend use of non-pharmacological interventions as first line treatment for distress, but further research is required to elucidate the components that lead to improved care for people living with dementia. This study aims to explore what works, examining case studies in which a non-pharmacological clinical intervention, the Newcastle Model, was used to understand and manage distressed behaviour in dementia care within care home settings. Method: A qualitative case study design was used. Three cases were selected from the Edinburgh Behaviour Support Service for their success in preventing care home placement breakdown during a distressed behaviour intervention in NHS Scotland. Family members and staff involved in the interventions within these cases were interviewed (N = 6). Thematic analysis was used to analyse data. Findings: All participants reported positive outcomes from the intervention. Three key themes were identified, each with subthemes. Participants described a supportive, non-judgmental environment which allowed them to integrate knowledge about dementia and tailor interventions to the specific needs of the individual living with dementia. There was also a sense of family and staff coming together to unite with shared goals. A preliminary model of all of themes and their interactions is presented. Conclusion: The study supports use of biopsychosocial, formulation-led approaches in the understanding and treatment of complex behavioural presentations in community care settings. It suggests that clinicians should endeavour to facilitate safe and open environments for care home staff and family members, in order to promote attribution change and person-centered care, and to help mediate differences and conflict between staff and family members.

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